Tag: M.W:100-200

Related Products of 127978-70-5 , The common heterocyclic compound, 127978-70-5, name is (5-Methoxypyridine-2-yl)methanol, molecular formula is C7H9NO2, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route.

5-methoxypyridine-2-carbaldehyde: To a solution of 5.7g (41 mmol) (5-methoxypyridin-2~ yl)methanol in 100 mL CHC I3 was added 15g MnO2 and the mixture heated to reflux for 2 hours, filtered, and washed with boiling CHCI3. The filtrate was washed with brine, dried over MgSO4, and concentrated in vacuo to afford 5-methoxypyridine-2-carbaldehyde as a white solid. IH NMR (400MHz5 CDCl3) delta 9.99 (s, IH), 8.44 (d, J=2.4Hz, IH), 7.97 (d, J=8.4Hz, IH), 7.3 (dd, J=8.4, 2.4Hz, IH), 3.95 (s, 2H)

The synthetic route of 127978-70-5 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; MERCK & CO., INC.; WO2007/120729; (2007); A2;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 103041-38-9, name is Ethyl 3-(pyridin-2-ylamino)propanoate. This compound has unique chemical properties. The synthetic route is as follows. Formula: C10H14N2O2

obtained in Step 1 19.3g (0.098mol) of Compound 2 was added to the reaction flask was added 100ml of ethyl acetate, taking 22.8g (0.12mol) N-2 -B- alanine ethyl ester pyridine i.e. compound 3, was dissolved in 50ml of ethyl acetate was added to the reaction solution, 25 stirred for 12h, the solvent was distilled off under reduced pressure (vacuum degree: 0.075Mpa; temperature: 50 ) to give a solid, 65 deg.] C, and dried under vacuum 0.08Mpa 2h, was 28.9g3- [4-methoxy-3-methyl -N- (2- pyridyl) – benzamido] – acrylic acid ethyl ester, compound 4 in a yield of 80.7%

With the rapid development of chemical substances, we look forward to future research findings about 103041-38-9.

Reference:
Patent; Kaifeng Baiyun Pharmacy Limited Company; Lin, hengbiao; zhu, zanmei; mao, ying; liu, zhiqing; li, yunduo; (8 pag.)CN105481831; (2016); A;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Application of 30563-98-5, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 30563-98-5, name is Ethyl 5-nitropicolinate. This compound has unique chemical properties. The synthetic route is as follows.

A suspension of 5-nitro-pyridine-2-carboxylic acid ethyl ester (2.00 g, 10.2 mmol) and 10% Pd/C (200 mg) in ethanol (30 [ML)] was shaken under hydrogen at 40 psi for 4 h. The catalyst was filtered onto Celite and rinsed. The filtrate was concentrated in vacuo to give 1.47 g (87% yield) of a yellow solid, which displayed [A’H] NMR that matched the literature (Min, R. S.; Aksenov, V. S. [CITEZ.] [HETEROCYCL. COMPD. (ENGL. TRANSL.)] 1988,24, 885-886) and was used without any further purification.

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 30563-98-5, Ethyl 5-nitropicolinate.

Reference:
Patent; PFIZER INC.; WO2004/14904; (2004); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Reference of 1034667-22-5, In the chemical reaction process,reaction time,type of solvent,can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product.An updated downstream synthesis route of 1034667-22-5 as follows.

Formation of 3-bromo-5-fluoro-lH-pyrazolo[3,4-Z>] pyridine (4)To a mixture of 5-fluoro-lH-pyrazolo[3,4-0]pyridin-3-arnine, 3, (0.88 g, 5.79 mmol) in bromoform (8.8 mL) was added /eri-butyl nitrite (1.38 mL, 1 1.57 mmol). This mixture was heated to 61 C for 1 h and then heated to 90 C for an additional hour. The mixture was cooled to room temperature and bromoform was removed under reduced pressure. The resulting crude – residue was purified by silica gel chromatography (5-50% ethyl acetate/hexanes) to afford 970 mg of the desired product as a white solid: NMR (300 MHz, DMSO-i/6) delta 14.22 (s, 1 H), 8.67 (dd, J = 2.7, 1.9 Hz, 1 H), 8.07 (dd, J = 8.2, 2.7 Hz, 1 H); LCMS Gradient 10-90%, 0.1% formic acid, 5min, C18/ACN, Retention Time = 2.42 min (M+H) 216.1 1.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,1034667-22-5, its application will become more common.

Reference:
Patent; VERTEX PHARMACEUTICALS INCORPORATED; CHARIFSON, Paul, S.; CLARK, Michael, P.; DAVIES, Ioana; GAO, Huai; KENNEDY, Joseph, M.; LEDEBOER, Mark, W.; MALTAIS, Francois; PEROLA, Emanuele; WO2012/83121; (2012); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Related Products of 881-86-7, As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 881-86-7, name is Dimethyl pyridine-2,5-dicarboxylate, molecular formula is C9H9NO4, The compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below.

Pyridine 2,5-dicarboxylic acid 5-methyl ester. Pyridine 2,5-dicarboxylic acid 5-methyl ester was synthesised according to the procedure described by Faul, M. M., et al., (J. Org. Chem. 66, 5772-5782, 2002). Di-ester (28 g, 0.146 moles) and methanol (260 mL) were stirred in a 500 mL 3-neck round bottom flask with connected a condenser and a funnel. The reaction mixture was heated at reflux after adding one portion of NaOH (6.2 g, 0.155 moles) for 3 h 30 min to produce a white mixture. While at reflux, 2M HCl (121 mL) was added dropwise over a 1 h period to produce a yellow solution. The flask was placed in an ice water bath to cool, and at r.t., a precipitate appears. The precipitate was collected by filtration and washed with 2:1 MeOH/H2O (35 mL) and then water (50 mL). The precipitate was dried overnight. The final yield was 19.68 g (75percent). NMR 1H 300 MHz, DMSO-d6 (delta, ppm): 9.12 (m, 1H), 8.40 (dd, J=2.1 Hz and 8.1 Hz, 1H, CH), 8.12 (dd, J=0.9 Hz and 8.4 Hz, 1H, CH), 3.89 (s, 3H, CH3). NMR 13C 75.45 MHz, DMSO-d6 (delta, ppm): 165.9, 165.0, 152.1, 150.2, 138.8, 128.3, 125.0, 53.2.

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 881-86-7, Dimethyl pyridine-2,5-dicarboxylate.

Reference:
Patent; Washington, University of; US2008/103192; (2008); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Electric Literature of 1060811-62-2, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 1060811-62-2, name is 4,6-Dichloronicotinaldehyde. This compound has unique chemical properties. The synthetic route is as follows.

To a stirred solution of 2,6-difluoro-3,5-dimethoxyaniline (9.03 g, 47.7 mmol), sodium triacetoxyborohydride (38.0 g, 180 mmol) in methylene chloride (60 mL)/trifluoroacetic acid (30. mL) at room temperature was added slowly a solution of 4,6-dichloronicotinaldehyde (8.00 g, 45.5 mmol) in methylene chloride (10 mL). After stirring at room temperature for 1 hour, the reaction mixture was concentrated under vacuo then saturated aqueous NaHCO3 (200 mL) was added. The resulting mixture was extracted with DCM (3×150 mL). The organic layers were combined, dried over Na2SO4, and concentrated. The residue was purified on silica gel (eluting with 0 to 40percent EtOAc in hexanes) to afford the desired product. LC-MS calculated for C14H13Cl2F2N2O2[M+H]+ m/z: 349.0. found 349.1.

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 1060811-62-2, 4,6-Dichloronicotinaldehyde.

Reference:
Patent; Incyte Corporation; Wu, Liangxing; Lu, Liang; Qian, Ding-Quan; Shen, Bo; Yao, Wenqing; (40 pag.)US2016/115164; (2016); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 65156-94-7, name is 5-Chloro-1H-pyrrolo[3,2-b]pyridine. This compound has unique chemical properties. The synthetic route is as follows. COA of Formula: C7H5ClN2

A mixture of 5-chloro-lH-pyrrolo[3,2-b]pyridine (450 mg, 2.95 mmol, 1 equiv), (1344) CS2CO3 (960.9 mg, 2.95 mmol, 1 equiv) and iodomethane (418.6 mg, 2.95 mmol, 1.000 equiv) in DMF (11.2 mL), was stirred for 4 h at 60 C. The reaction was quenched by the addition of 30 mL of water, extracted with 10 ml of ethyl acetate and the combined organic layers concentrated under reduced pressure. The residue was purified by silica gel chromatography with ethyl acetate/petroleum ether (1 : 10) as eluent to afford the desired final product as a yellow oil in 81% yield.

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it, 65156-94-7, 5-Chloro-1H-pyrrolo[3,2-b]pyridine.

Reference:
Patent; IDEAYA BIOSCIENCES, INC.; ALAM, Muzaffar; ASWAD, Fred; BECK, Hilary Plake; DILLON, Michael Patrick; GONZALEZ-LOPEZ, Marcos; HATA, Yujiro; RICO, Alice Chen; SUTTON, JR., James Clifford; (342 pag.)WO2020/18848; (2020); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Reference of 6298-19-7, Adding some certain compound to certain chemical reactions, such as: 6298-19-7, name is 2-Chloropyridin-3-amine,molecular formula is C5H5ClN2, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 6298-19-7.

12.8 g of 2-chloro-3-aminopyridine was suspended in 120 mL of 60% aqueous hexafluorophosphoric acid, and 9.0 g sodium nitrite was added little by little thereto at 0C to precipitate crystals. The crystals were collected by filtration and washed with diethyl ether to give 15.75 g diazonium salt. Subsequently, the diazonium salt was suspended in 100 mL xylene and heated at 85C for 3 hours, 28 mL triethylamine was added thereto, and the reaction mixture was diluted with an aqueous saturated sodium bicarbonatesolution and then extracted with ethyl acetate. The extract was washed with brine, and the organic layer was dried over anhydrous sodium sulfate and then filtered through silica gel. The ethyl acetate was removed, and to the resulting xylene solution was added 6.0 mL 2-aminoethanol, and the mixture was heated at 130C for 10 hours. Then, the same procedure as in Production Example 231 was carried out, whereby 385 mg of the title compound (yellowoil) was obtained as a mixture.1H-NMR (CDCl3) delta: 3.60-3.68(m, 2H), 3.84(t, J=4.8Hz, 2H), 6.52-6.60(m, 1H), 7.12-7.20(m, 1H), 7.80-7.85(m, 1H)

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles. 6298-19-7, 2-Chloropyridin-3-amine, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Eisai Co., Ltd.; EP1382603; (2004); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Reference of 1539-42-0 , The common heterocyclic compound, 1539-42-0, name is Bis(pyridin-2-ylmethyl)amine, molecular formula is C12H13N3, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route.

Di-(2-picolyl)amine (5.0 mmol, 900 muL)was dissolved in THF (10 mL). K2CO3 (20 mmol, 2.76 g) wasadded followed by dropwise addition of propargyl bromide (80% in toluene, 5.0mmol, 557 muL). The reaction mixture was stirred for 16 hrs before diluted withDCM. The diluted reaction mixture was filtrated through a pad of K2CO3under vacuum before concentrated. Compound 2was isolated in 96% yield from an alumina column elutedby EtOAc in DCM (0% – 40%). 1H-NMR(500 MHz, CDCl3, ppm) delta = 8.52(m, 2H), 7.62 (td, J = 2.0, 7.5 Hz, 2H), 7.47 (d, J= 8.0 Hz, 2H), 7.12 (td, J = 1.0, 5.0Hz, 2H), 3.88 (s, 4H), 3.37 (d, J =2.0 Hz, 2H), 2.27 (t, J = 2.5 Hz,1H); 13C-NMR (125 MHz, CDCl3,ppm) delta =153.6, 129.6, 83.6, 45.2, 34.6, 32.3, 26.5, 24.9.

The synthetic route of 1539-42-0 has been constantly updated, and we look forward to future research findings.

Reference:
Article; Yao, Zi-Jian; Hong, Shibin; Zhang, Wei; Liu, Mengyan; Deng, Wei; Tetrahedron Letters; vol. 57; 8; (2016); p. 910 – 913;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Related Products of 73027-79-9, Adding some certain compound to certain chemical reactions, such as: 73027-79-9, name is 4,6-Dichloronicotinic acid,molecular formula is C6H3Cl2NO2, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 73027-79-9.

To a solution of 4,6-dichloronicotinic acid (300 mg) in N,N-dimethylacetamide (4.0 mL) were added 2-(7-azabenzotriazol-1-yl)-1,1,3,3-hexafluorophosphate (HATU) (0.89 g), diisopropylethylamine (0.55 mL) and dimethylamine hydrochloride (190 mg), and the mixture was stirred overnight at room temperature. The reaction mixture was cooled to 0 C., saturated aqueous sodium hydrogencarbonate solution was added thereto, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed successively with water and saturated brine, and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (hexane/ethyl acetate) to give the title compound (240 mg). MS(ESI+): [M+H]+ 218.7.

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles. 73027-79-9, 4,6-Dichloronicotinic acid, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; TAKEDA PHARMACEUTICAL COMPANY LIMITED; Saitoh, Morihisa; Yogo, Takatoshi; Kamei, Taku; Tokunaga, Norihito; Ohba, Yusuke; Yukawa, Takafumi; (191 pag.)US2016/159773; (2016); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem